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The reaction sequence shows how CH₃CH₂ can be converted into BrCH₂CH₂Br CH₃CH₃ + Cl₂ → Step A NaOH → Step B CH₃CH₂OH → Step C BrCH₂CH₂Br + Br₂ → Step D Which step occurs by nucleophilic substitution? - AQA - A-Level Chemistry - Question 14 - 2017 - Paper 3

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Question 14

The-reaction-sequence-shows-how-CH₃CH₂-can-be-converted-into-BrCH₂CH₂Br--CH₃CH₃-+-Cl₂-→-Step-A-NaOH-→-Step-B-CH₃CH₂OH-→-Step-C-BrCH₂CH₂Br-+-Br₂-→-Step-D--Which-step-occurs-by-nucleophilic-substitution?-AQA-A-Level Chemistry-Question 14-2017-Paper 3.png

The reaction sequence shows how CH₃CH₂ can be converted into BrCH₂CH₂Br CH₃CH₃ + Cl₂ → Step A NaOH → Step B CH₃CH₂OH → Step C BrCH₂CH₂Br + Br₂ → Step D Which step ... show full transcript

Worked Solution & Example Answer:The reaction sequence shows how CH₃CH₂ can be converted into BrCH₂CH₂Br CH₃CH₃ + Cl₂ → Step A NaOH → Step B CH₃CH₂OH → Step C BrCH₂CH₂Br + Br₂ → Step D Which step occurs by nucleophilic substitution? - AQA - A-Level Chemistry - Question 14 - 2017 - Paper 3

Step 1

Step A

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Answer

Step A involves the reaction of ethane (CH₃CH₃) with chlorine (Cl₂) in a halogenation reaction, which is not a nucleophilic substitution.

Step 2

Step B

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Answer

Step B is where sodium hydroxide (NaOH) reacts with CH₃CH₂Cl (ethyl chloride). This reaction is a classic example of nucleophilic substitution (S_N2) as the hydroxide ion acts as a nucleophile, replacing the chlorine atom.

Step 3

Step C

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Answer

Step C involves the alcohol formation where CH₃CH₂OH does not involve nucleophilic substitution but rather involves proton transfer.

Step 4

Step D

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Answer

Step D is the bromination of dibromide, which does not involve nucleophilic substitution either.

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